Alendronate sodium and Post procedural constipation - a phase IV clinical study of FDA data

Summary:

Post procedural constipation is reported as a side effect among people who take Alendronate sodium (alendronate sodium), especially for people who are female, 60+ old, have been taking the drug for 6 - 12 months also take Fosamax, and have High blood pressure.

The phase IV clinical study analyzes which people have Post procedural constipation when taking Alendronate sodium. It is created by eHealthMe based on reports of 42,896 people who have side effects when taking Alendronate sodium from the FDA, and is updated regularly.

What is Alendronate sodium?

Alendronate sodium has active ingredients of alendronate sodium. It is often used in osteoporosis. eHealthMe is studying from 43,608 Alendronate sodium users. Check the latest studies of Alendronate sodium.

What is Post procedural constipation?

Post procedural constipation is found to be associated with 22 drugs and 77 conditions by eHealthMe. Check the latest studies of Post procedural constipation.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Aug, 30, 2026

42,896 people reported to have side effects when taking Alendronate sodium.
Among them, 26 people (0.06%) have Post procedural constipation.

Could Alendronate sodium cause Post procedural constipation?

Among these 26 people:

How long have people been on Alendronate sodium when they have Post procedural constipation? *

What is the gender of people who have Post procedural constipation when taking Alendronate sodium? *

female: 92.31 %
male: 7.69 %

What is the age of people who have Post procedural constipation when taking Alendronate sodium? *

What are other drugs people take besides Alendronate sodium? *

Fosamax: 26 people, 100.00%
Vitamins: 7 people, 26.92%
Azor: 5 people, 19.23%
Boniva: 2 people, 7.69%

What are other side effects people have besides Post procedural constipation? *

Femur Fracture: 26 people, 100.00%
Anaemia Postoperative: 24 people, 92.31%
Fall: 23 people, 88.46%
High Blood Pressure: 19 people, 73.08%
Low Turnover Osteopathy (slow removal of old bone and its replacement by new bone): 19 people, 73.08%
High Blood Cholesterol: 18 people, 69.23%
Hyperlipidaemia (presence of excess lipids in the blood): 14 people, 53.85%
Osteoarthritis (a joint disease caused by cartilage loss in a joint): 13 people, 50.00%
Broken Bone: 12 people, 46.15%
Bursitis (inflammation of a bursa, typically one in the knee, elbow, or shoulder): 12 people, 46.15%

What are the existing conditions these people have? *

High Blood Pressure: 5 people, 19.23%
Bone Disorder: 2 people, 7.69%

* Approximation only. Some reports may have incomplete information.

Do you take Alendronate sodium and have Post procedural constipation?

- Check whether Post procedural constipation is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Alendronate sodium:

Alendronate sodium (43,608 reports)

Browse all side effects of Alendronate sodium:

a b c d e f g h i j k l m n o p q r s t u v w x y z

Browse all the drugs that are associated with Post procedural constipation:

Post procedural constipation (22 drugs)

Browse all the conditions that are associated with Post procedural constipation:

Post procedural constipation (77 conditions)

Related publications that referenced our studies

Stuckey BG, Sallie R, "Alendronate-induced unmasking or deterioration of coeliac disease: a case series", Osteoporosis International, 2015 Jan .
Lee WY, Sun LM, Lin MC, Liang JA, Chang SN, Sung FC, Muo CH, Kao CH, "A higher dosage of oral alendronate will increase the subsequent cancer risk of osteoporosis patients in Taiwan: a population-based cohort study", PloS one, 2012 Dec .
Stuckey BG, Sallie R, "Alendronate-induced unmasking or deterioration of coeliac disease: a case series", Osteoporosis International, 2015 Jan .
Lee WY, Sun LM, Lin MC, Liang JA, Chang SN, Sung FC, Muo CH, Kao CH, "A higher dosage of oral alendronate will increase the subsequent cancer risk of osteoporosis patients in Taiwan: a population-based cohort study", PloS one, 2012 Dec .

How the study uses the data?

The study uses data from the FDA. It is based on alendronate sodium (the active ingredients of Alendronate sodium) and Alendronate sodium (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.

How to use the study?

DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.

Who is eHealthMe?

With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only. Our phase IV clinical studies alone cannot establish cause-effect relationship. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.